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4-IODOTHIOBENZAMIDE

Base Information Edit
  • Chemical Name:4-IODOTHIOBENZAMIDE
  • CAS No.:106748-23-6
  • Molecular Formula:C7H6INS
  • Molecular Weight:263.102
  • Hs Code.:
  • Mol file:106748-23-6.mol
4-IODOTHIOBENZAMIDE

Synonyms:4-iodobenzothioamide

Suppliers and Price of 4-IODOTHIOBENZAMIDE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • SynQuest Laboratories
  • 4-Iodothiobenzamide 98%
  • 5 g
  • $ 269.00
  • SynQuest Laboratories
  • 4-Iodothiobenzamide 98%
  • 1 g
  • $ 95.00
  • Matrix Scientific
  • 4-Iodothiobenzamide 98%
  • 1g
  • $ 90.00
  • Matrix Scientific
  • 4-Iodothiobenzamide 98%
  • 10g
  • $ 600.00
  • Matrix Scientific
  • 4-Iodothiobenzamide 98%
  • 5g
  • $ 349.00
  • AHH
  • 4-IODOTHIOBENZAMIDE 97%
  • 10g
  • $ 330.00
Total 5 raw suppliers
Chemical Property of 4-IODOTHIOBENZAMIDE Edit
Chemical Property:
  • Melting Point:164~165℃ (dec) 
Purity/Quality:

97% *data from raw suppliers

4-Iodothiobenzamide 98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 4-IODOTHIOBENZAMIDE

There total 4 articles about 4-IODOTHIOBENZAMIDE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With Lawessons reagent; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/j.bmcl.2021.127853
Guidance literature:
With 2,3,4,5,7,8,9,10-octahydropyrimido[1,2-a]azepin-1-ium acetate; sodiumsulfide nonahydrate; In neat (no solvent); at 20 ℃; for 2h; Green chemistry;
DOI:10.1039/c7ra11259a
Guidance literature:
Multi-step reaction with 2 steps
1.1: thionyl chloride / 2 h / Reflux
1.2: 20 °C
2.1: Lawessons reagent / tetrahydrofuran / 20 °C
With Lawessons reagent; thionyl chloride; In tetrahydrofuran;
DOI:10.1016/j.bmcl.2021.127853
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